Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_assertion description "[Mutations in the NPHS1 and NPHS2 genes are among the main causes of early-onset and familial steroid resistant nephrotic syndrome respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_assertion evidence source_evidence_literature NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_assertion SIO_000772 22565185 NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_assertion wasDerivedFrom befree-2016 NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_assertion wasGeneratedBy ECO_0000203 NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.
- befree-2016 importedOn "2016-02-19" NP980277.RAsGs04-Tjnxqig24FRDQUofSTE9AiOQZViyYJpIolARs130_provenance.